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PRECICE® Intramedullary Limb Lengthening System P003Recalls & reported problems

Nuvasive Specialized Orthopedics, Inc. · ERC1, PRECICE, Shipping Pkg EU · Class 2

All models of PRECICE Intramedullary Limb Lengthening System (551)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00856719002060), received between Dec 10, 2019 and Dec 10, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Defective Device” (2 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Defective Device2

Patient problems

  • No Code Available2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 10, 2019Defective Device; Defective Device

    INFORMATION WAS RECEIVED THAT THE PATIENT WAS EXPERIENCING A LOSS OF DISTRACTION.

    Patient problems: No Code Available

    MAUDE report 9446221 ↗
  • MalfunctionDec 10, 2019Defective Device; Defective Device

    INFORMATION WAS RECEIVED THAT THE PATIENT WAS EXPERIENCING A LOSS OF DISTRACTION.

    Patient problems: No Code Available

    MAUDE report 9446109 ↗

Other Rod, Fixation, Intramedullary And Accessories devices

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Sources and updates

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